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Mitochondrial bioenergetics and D-ribose in HFpEF: a brief narrative review

OBJECTIVE: In this review article, we briefly describe the status of treatment options for HFpEF and the role of mitochondrial dysfunction in the pathogenesis of HFpEF as an alternative therapeutic target. We also examine the mechanisms of D-ribose in cellular energy production and discuss the poten...

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Autores principales: Krueger, Kathryn J., Rahman, Faith K., Shen, Qiuhua, Vacek, James, Hiebert, John B., Pierce, Janet D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8573443/
https://www.ncbi.nlm.nih.gov/pubmed/34805366
http://dx.doi.org/10.21037/atm-21-2291
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author Krueger, Kathryn J.
Rahman, Faith K.
Shen, Qiuhua
Vacek, James
Hiebert, John B.
Pierce, Janet D.
author_facet Krueger, Kathryn J.
Rahman, Faith K.
Shen, Qiuhua
Vacek, James
Hiebert, John B.
Pierce, Janet D.
author_sort Krueger, Kathryn J.
collection PubMed
description OBJECTIVE: In this review article, we briefly describe the status of treatment options for HFpEF and the role of mitochondrial dysfunction in the pathogenesis of HFpEF as an alternative therapeutic target. We also examine the mechanisms of D-ribose in cellular energy production and discuss the potential disadvantages and benefits of supplemental use of D-ribose in patients with HFpEF. BACKGROUND: Heart failure is a major cardiovascular disease that impacts over 6 million Americans and is one of the leading causes for morbidity and mortality. Patients with heart failure often experience shortness of breath and fatigue along with impaired physical capacity, all leading to poor quality of life. As a subtype of heart failure, heart failure with preserved ejection fraction (HFpEF) is characterized with impaired diastolic function. Currently, there are no effective treatments specifically for HFpEF, thus clinicians and researchers are searching for therapies to improve cardiac function. Emerging evidence indicate that mitochondrial dysfunction and impaired cardiac bioenergetics are among the underlying mechanisms for HFpEF. There is increased interest in investigating the use of supplements such as D-ribose to enhance mitochondrial function and improve production of adenosine triphosphate (ATP). METHODS: For this narrative review, more than 100 relevant scientific articles were considered from various databases (e.g., PubMed, Web of Science, CINAHL, and Google Scholar) using the keywords “Heart Failure”, “HFpEF”, “D-ribose”, “ATP”, “Mitochondria”, Bioenergetics”, and “Cellular Respiration”. CONCLUSIONS: It is essential to find potential targeted therapeutic treatments for HFpEF. Since there is evidence that the HFpEF is related to impaired myocardial bioenergetics, enhancing mitochondrial function could augment cardiac function. Using a supplement such as D-ribose could improve mitochondrial function by increasing ATP and enhancing cardiac performance for patients with HFpEF. There is a recently completed clinical trial with HFpEF patients that indicates D-ribose increases ATP production and improves cardiac ejection fraction.
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spelling pubmed-85734432021-11-18 Mitochondrial bioenergetics and D-ribose in HFpEF: a brief narrative review Krueger, Kathryn J. Rahman, Faith K. Shen, Qiuhua Vacek, James Hiebert, John B. Pierce, Janet D. Ann Transl Med Review Article OBJECTIVE: In this review article, we briefly describe the status of treatment options for HFpEF and the role of mitochondrial dysfunction in the pathogenesis of HFpEF as an alternative therapeutic target. We also examine the mechanisms of D-ribose in cellular energy production and discuss the potential disadvantages and benefits of supplemental use of D-ribose in patients with HFpEF. BACKGROUND: Heart failure is a major cardiovascular disease that impacts over 6 million Americans and is one of the leading causes for morbidity and mortality. Patients with heart failure often experience shortness of breath and fatigue along with impaired physical capacity, all leading to poor quality of life. As a subtype of heart failure, heart failure with preserved ejection fraction (HFpEF) is characterized with impaired diastolic function. Currently, there are no effective treatments specifically for HFpEF, thus clinicians and researchers are searching for therapies to improve cardiac function. Emerging evidence indicate that mitochondrial dysfunction and impaired cardiac bioenergetics are among the underlying mechanisms for HFpEF. There is increased interest in investigating the use of supplements such as D-ribose to enhance mitochondrial function and improve production of adenosine triphosphate (ATP). METHODS: For this narrative review, more than 100 relevant scientific articles were considered from various databases (e.g., PubMed, Web of Science, CINAHL, and Google Scholar) using the keywords “Heart Failure”, “HFpEF”, “D-ribose”, “ATP”, “Mitochondria”, Bioenergetics”, and “Cellular Respiration”. CONCLUSIONS: It is essential to find potential targeted therapeutic treatments for HFpEF. Since there is evidence that the HFpEF is related to impaired myocardial bioenergetics, enhancing mitochondrial function could augment cardiac function. Using a supplement such as D-ribose could improve mitochondrial function by increasing ATP and enhancing cardiac performance for patients with HFpEF. There is a recently completed clinical trial with HFpEF patients that indicates D-ribose increases ATP production and improves cardiac ejection fraction. AME Publishing Company 2021-10 /pmc/articles/PMC8573443/ /pubmed/34805366 http://dx.doi.org/10.21037/atm-21-2291 Text en 2021 Annals of Translational Medicine. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Review Article
Krueger, Kathryn J.
Rahman, Faith K.
Shen, Qiuhua
Vacek, James
Hiebert, John B.
Pierce, Janet D.
Mitochondrial bioenergetics and D-ribose in HFpEF: a brief narrative review
title Mitochondrial bioenergetics and D-ribose in HFpEF: a brief narrative review
title_full Mitochondrial bioenergetics and D-ribose in HFpEF: a brief narrative review
title_fullStr Mitochondrial bioenergetics and D-ribose in HFpEF: a brief narrative review
title_full_unstemmed Mitochondrial bioenergetics and D-ribose in HFpEF: a brief narrative review
title_short Mitochondrial bioenergetics and D-ribose in HFpEF: a brief narrative review
title_sort mitochondrial bioenergetics and d-ribose in hfpef: a brief narrative review
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8573443/
https://www.ncbi.nlm.nih.gov/pubmed/34805366
http://dx.doi.org/10.21037/atm-21-2291
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